UNFOLDER SILVER SILVERT

GUDID 15050474523491

SILVER SERIES HANDPIECE (TWIST)

JOHNSON & JOHNSON SURGICAL VISION, INC.

Manual intraocular lens injector, reusable Manual intraocular lens injector, reusable Manual intraocular lens injector, reusable Manual intraocular lens injector, reusable Manual intraocular lens injector, reusable Manual intraocular lens injector, reusable Manual intraocular lens injector, reusable Manual intraocular lens injector, reusable Manual intraocular lens injector, reusable Manual intraocular lens injector, reusable Manual intraocular lens injector, reusable Manual intraocular lens injector, reusable Manual intraocular lens injector, reusable Manual intraocular lens injector, reusable Manual intraocular lens injector, reusable Manual intraocular lens injector, reusable Manual intraocular lens injector, reusable Manual intraocular lens injector, reusable Manual intraocular lens injector, reusable Manual intraocular lens injector, reusable Manual intraocular lens injector, reusable Manual intraocular lens injector, reusable Manual intraocular lens injector, reusable Manual intraocular lens injector, reusable Manual intraocular lens injector, reusable Manual intraocular lens injector, reusable Manual intraocular lens injector, reusable

• Primary Device ID: 15050474523491
• NIH Device Record Key: b70b10fd-3a5b-4358-b16d-d03e24710061
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: UNFOLDER SILVER
• Version Model Number: SILVERT
• Catalog Number: SILVERT
• Company DUNS: 103021940
• Company Name: JOHNSON & JOHNSON SURGICAL VISION, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(877)266-4543
• Email: JJV-US-SURGICALORDERS@ITS.JNJ.COM
• Phone: +1(877)266-4543
• Email: JJV-US-SURGICALORDERS@ITS.JNJ.COM
• Phone: +1(877)266-4543
• Email: JJV-US-SURGICALORDERS@ITS.JNJ.COM
• Phone: +1(877)266-4543
• Email: JJV-US-SURGICALORDERS@ITS.JNJ.COM
• Phone: +1(877)266-4543
• Email: JJV-US-SURGICALORDERS@ITS.JNJ.COM
• Phone: +1(877)266-4543
• Email: JJV-US-SURGICALORDERS@ITS.JNJ.COM
• Phone: +1(877)266-4543
• Email: JJV-US-SURGICALORDERS@ITS.JNJ.COM
• Phone: +1(877)266-4543
• Email: JJV-US-SURGICALORDERS@ITS.JNJ.COM
• Phone: +1(877)266-4543
• Email: JJV-US-SURGICALORDERS@ITS.JNJ.COM
• Phone: +1(877)266-4543
• Email: JJV-US-SURGICALORDERS@ITS.JNJ.COM
• Phone: +1(877)266-4543
• Email: JJV-US-SURGICALORDERS@ITS.JNJ.COM
• Phone: +1(877)266-4543
• Email: JJV-US-SURGICALORDERS@ITS.JNJ.COM
• Phone: +1(877)266-4543
• Email: JJV-US-SURGICALORDERS@ITS.JNJ.COM
• Phone: +1(877)266-4543
• Email: JJV-US-SURGICALORDERS@ITS.JNJ.COM
• Phone: +1(877)266-4543
• Email: JJV-US-SURGICALORDERS@ITS.JNJ.COM
• Phone: +1(877)266-4543
• Email: JJV-US-SURGICALORDERS@ITS.JNJ.COM
• Phone: +1(877)266-4543
• Email: JJV-US-SURGICALORDERS@ITS.JNJ.COM
• Phone: +1(877)266-4543
• Email: JJV-US-SURGICALORDERS@ITS.JNJ.COM
• Phone: +1(877)266-4543
• Email: JJV-US-SURGICALORDERS@ITS.JNJ.COM
• Phone: +1(877)266-4543
• Email: JJV-US-SURGICALORDERS@ITS.JNJ.COM
• Phone: +1(877)266-4543
• Email: JJV-US-SURGICALORDERS@ITS.JNJ.COM
• Phone: +1(877)266-4543
• Email: JJV-US-SURGICALORDERS@ITS.JNJ.COM
• Phone: +1(877)266-4543
• Email: JJV-US-SURGICALORDERS@ITS.JNJ.COM
• Phone: +1(877)266-4543
• Email: JJV-US-SURGICALORDERS@ITS.JNJ.COM
• Phone: +1(877)266-4543
• Email: JJV-US-SURGICALORDERS@ITS.JNJ.COM
• Phone: +1(877)266-4543
• Email: JJV-US-SURGICALORDERS@ITS.JNJ.COM
• Phone: +1(877)266-4543
• Email: JJV-US-SURGICALORDERS@ITS.JNJ.COM

Device Identifiers

Device Issuing Agency	Device ID
GS1	15050474523491 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K961242

FDA Product Code

• KYB: LENS, GUIDE, INTRAOCULAR

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: true

[15050474523491]

Moist Heat or Steam Sterilization

[15050474523491]

Moist Heat or Steam Sterilization

[15050474523491]

Moist Heat or Steam Sterilization

[15050474523491]

Moist Heat or Steam Sterilization

[15050474523491]

Moist Heat or Steam Sterilization

[15050474523491]

Moist Heat or Steam Sterilization

[15050474523491]

Moist Heat or Steam Sterilization

[15050474523491]

Moist Heat or Steam Sterilization

[15050474523491]

Moist Heat or Steam Sterilization

[15050474523491]

Moist Heat or Steam Sterilization

[15050474523491]

Moist Heat or Steam Sterilization

[15050474523491]

Moist Heat or Steam Sterilization

[15050474523491]

Moist Heat or Steam Sterilization

[15050474523491]

Moist Heat or Steam Sterilization

[15050474523491]

Moist Heat or Steam Sterilization

[15050474523491]

Moist Heat or Steam Sterilization

[15050474523491]

Moist Heat or Steam Sterilization

[15050474523491]

Moist Heat or Steam Sterilization

[15050474523491]

Moist Heat or Steam Sterilization

[15050474523491]

Moist Heat or Steam Sterilization

[15050474523491]

Moist Heat or Steam Sterilization

[15050474523491]

Moist Heat or Steam Sterilization

[15050474523491]

Moist Heat or Steam Sterilization

[15050474523491]

Moist Heat or Steam Sterilization

[15050474523491]

Moist Heat or Steam Sterilization

[15050474523491]

Moist Heat or Steam Sterilization

[15050474523491]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2020-02-26
• Device Publish Date: 2019-02-13

On-Brand Devices [UNFOLDER SILVER]

• 15050474530031: SILVER CARTRIDGE THERMOFORMED TR, 30 BX
• 15050474523491: SILVER SERIES HANDPIECE (TWIST)